Kifayat Sumaiya, Almuqdadi Haider Thaer Abdulhameed, Singh Ravindra Pal, Singh Mithilesh, Abid Mohammad, Sanapalli Bharat Kumar Reddy
Department of Pharmacology, NIMS Institute of Pharmacy, NIMS University Rajasthan, Jaipur, 303121, India.
Medicinal Chemistry Laboratory, Department of Biosciences, Jamia Millia Islamia, Jamia Nagar, New Delhi, 110025, India.
Mol Divers. 2024 Dec;28(6):3937-3948. doi: 10.1007/s11030-023-10787-4. Epub 2024 May 22.
The remarkable conservation of the FtsZ among Gram-positive and Gram-negative bacteria, a crucial GTPase in bacterial cell division, has emerged as a promising antibacterial drug target to combat antibacterial resistance. There have been several coordinated efforts to develop inhibitors against FtsZ which can also serve as potential candidates for future antibiotics. In the present study, a natural product-like library (≈50,000 compounds) was employed to conduct HTVS against Staphylococcus aureus FtsZ protein (PDB Id: 6KVP). Additionally, molecular docking was carried out in two modes, SP and XP docking, using the Schrödinger suite. The glide scores of ligands obtained by XP docking were further summarized and compared with the control ligands (ZI1- co-crystal and PC190723-a compound undergoing clinical trial). Using the Prime-MM-GBSA approach, BFE calculations were performed on the top XP-scored ligands (≈598 compounds). These hits were also evaluated for ADMET parameters using the Qikprop algorithm, SwissADME, and in silico carcinogenicity testing using Carcinopred-El. Based on the results, ligand 4-FtsZ complex was considered for the 300 ns MDS analysis to get insights into its binding modes within the catalytic pocket of FtsZ protein. The analysis revealed that the amide linkage sandwiched between the triazole and 1-oxa-8-azaspirodecan-8-ium moiety (Val203) as well as the aminoethyl group present at 1st position on the triazole moiety (Leu209, Leu200, Asp210, and Ala202) were responsible for the FtsZ inhibitory activity, owing to their crucial interactions with key amino acid residues. Further, the complex also displayed good protein-ligand stability, ultimately predicting ligand 4 as a potent lead compound for the inhibition of FtsZ. Thus, our in silico findings will serve as a framework for in-depth in-vitro and in-vivo investigations encouraging the development of FtsZ inhibitors as a new generation of antibacterial agents.
FtsZ在革兰氏阳性菌和革兰氏阴性菌中显著保守,它是细菌细胞分裂中的一种关键GTP酶,已成为对抗抗菌耐药性的一个有前景的抗菌药物靶点。已经有多项协同努力来开发针对FtsZ的抑制剂,这些抑制剂也可作为未来抗生素的潜在候选物。在本研究中,使用了一个类似天然产物的文库(约50,000种化合物)对金黄色葡萄球菌FtsZ蛋白(PDB编号:6KVP)进行高通量虚拟筛选(HTVS)。此外,使用薛定谔软件包以两种模式进行分子对接,即标准精度(SP)对接和额外精度(XP)对接。对通过XP对接获得的配体的Glide评分进行进一步汇总,并与对照配体(ZI1 - 共晶体和正在进行临床试验的化合物PC190723)进行比较。使用Prime - MM - GBSA方法,对得分最高的XP配体(约598种化合物)进行结合自由能(BFE)计算。还使用Qikprop算法、SwissADME对这些命中化合物的ADMET参数进行评估,并使用Carcinopred - El进行计算机致癌性测试。基于结果,选择配体4 - FtsZ复合物进行300纳秒的分子动力学模拟(MDS)分析,以深入了解其在FtsZ蛋白催化口袋内的结合模式。分析表明,夹在三唑和1 - 氧杂 - 8 - 氮杂螺癸烷鎓部分(Val203)之间的酰胺键以及三唑部分第1位的氨乙基(Leu209、Leu200、Asp210和Ala202)负责FtsZ抑制活性,这是由于它们与关键氨基酸残基的关键相互作用。此外,该复合物还表现出良好的蛋白质 - 配体稳定性,最终预测配体4是抑制FtsZ的有效先导化合物。因此,我们的计算机模拟结果将作为深入的体外和体内研究的框架,推动FtsZ抑制剂作为新一代抗菌剂的开发。